Canonical Allele Identifier: PA2573201814
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407592
ClinVar RCV Id: RCV001937829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317021.1:p.Asn209Ser
CA346820186
NM_001330092.2:c.626A>G